A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761076



Internal ID18735322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:105357082..105358874hg38UCSC Ensembl
Outerchr3:105356775..105359204hg38UCSC Ensembl
Innerchr3:105075926..105077718hg19UCSC Ensembl
Outerchr3:105075619..105078048hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg382430
hg192430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761076
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer